Cargando…

Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes

Brain metastasis is common in lung cancer, and treatment of brain metastasis can lead to significant morbidity. Although early detection of brain metastasis may improve outcomes, there are no prediction models to identify high-risk patients for brain magnetic resonance imaging (MRI) surveillance. Ou...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Julie, Ding, Victoria, Luo, Sophia, Choi, Eunji, Hellyer, Jessica, Myall, Nathaniel, Henry, Solomon, Wood, Douglas, Stehr, Henning, Ji, Hanlee, Nagpal, Seema, Hayden Gephart, Melanie, Wakelee, Heather, Neal, Joel, Han, Summer S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9848601/
https://www.ncbi.nlm.nih.gov/pubmed/36201713
http://dx.doi.org/10.1200/PO.22.00220
_version_ 1784871745666154496
author Wu, Julie
Ding, Victoria
Luo, Sophia
Choi, Eunji
Hellyer, Jessica
Myall, Nathaniel
Henry, Solomon
Wood, Douglas
Stehr, Henning
Ji, Hanlee
Nagpal, Seema
Hayden Gephart, Melanie
Wakelee, Heather
Neal, Joel
Han, Summer S.
author_facet Wu, Julie
Ding, Victoria
Luo, Sophia
Choi, Eunji
Hellyer, Jessica
Myall, Nathaniel
Henry, Solomon
Wood, Douglas
Stehr, Henning
Ji, Hanlee
Nagpal, Seema
Hayden Gephart, Melanie
Wakelee, Heather
Neal, Joel
Han, Summer S.
author_sort Wu, Julie
collection PubMed
description Brain metastasis is common in lung cancer, and treatment of brain metastasis can lead to significant morbidity. Although early detection of brain metastasis may improve outcomes, there are no prediction models to identify high-risk patients for brain magnetic resonance imaging (MRI) surveillance. Our goal is to develop a machine learning–based clinicogenomic prediction model to estimate patient-level brain metastasis risk. METHODS: A penalized regression competing risk model was developed using 330 patients diagnosed with lung cancer between January 2014 and June 2019 and followed through June 2021 at Stanford HealthCare. The main outcome was time from the diagnosis of distant metastatic disease to the development of brain metastasis, death, or censoring. RESULTS: Among the 330 patients, 84 (25%) developed brain metastasis over 627 person-years, with a 1-year cumulative brain metastasis incidence of 10.2% (95% CI, 6.8 to 13.6). Features selected for model inclusion were histology, cancer stage, age at diagnosis, primary site, and RB1 and ALK alterations. The prediction model yielded high discrimination (area under the curve 0.75). When the cohort was stratified by risk using a 1-year risk threshold of > 14.2% (85th percentile), the high-risk group had increased 1-year cumulative incidence of brain metastasis versus the low-risk group (30.8% v 6.1%, P < .01). Of 48 high-risk patients, 24 developed brain metastasis, and of these, 12 patients had brain metastasis detected more than 7 months after last brain MRI. Patients who missed this 7-month window had larger brain metastases (58% v 33% largest diameter > 10 mm; odds ratio, 2.80, CI, 0.51 to 13) versus those who had MRIs more frequently. CONCLUSION: The proposed model can identify high-risk patients, who may benefit from more intensive brain MRI surveillance to reduce morbidity of subsequent treatment through early detection.
format Online
Article
Text
id pubmed-9848601
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-98486012023-01-19 Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes Wu, Julie Ding, Victoria Luo, Sophia Choi, Eunji Hellyer, Jessica Myall, Nathaniel Henry, Solomon Wood, Douglas Stehr, Henning Ji, Hanlee Nagpal, Seema Hayden Gephart, Melanie Wakelee, Heather Neal, Joel Han, Summer S. JCO Precis Oncol ORIGINAL REPORTS Brain metastasis is common in lung cancer, and treatment of brain metastasis can lead to significant morbidity. Although early detection of brain metastasis may improve outcomes, there are no prediction models to identify high-risk patients for brain magnetic resonance imaging (MRI) surveillance. Our goal is to develop a machine learning–based clinicogenomic prediction model to estimate patient-level brain metastasis risk. METHODS: A penalized regression competing risk model was developed using 330 patients diagnosed with lung cancer between January 2014 and June 2019 and followed through June 2021 at Stanford HealthCare. The main outcome was time from the diagnosis of distant metastatic disease to the development of brain metastasis, death, or censoring. RESULTS: Among the 330 patients, 84 (25%) developed brain metastasis over 627 person-years, with a 1-year cumulative brain metastasis incidence of 10.2% (95% CI, 6.8 to 13.6). Features selected for model inclusion were histology, cancer stage, age at diagnosis, primary site, and RB1 and ALK alterations. The prediction model yielded high discrimination (area under the curve 0.75). When the cohort was stratified by risk using a 1-year risk threshold of > 14.2% (85th percentile), the high-risk group had increased 1-year cumulative incidence of brain metastasis versus the low-risk group (30.8% v 6.1%, P < .01). Of 48 high-risk patients, 24 developed brain metastasis, and of these, 12 patients had brain metastasis detected more than 7 months after last brain MRI. Patients who missed this 7-month window had larger brain metastases (58% v 33% largest diameter > 10 mm; odds ratio, 2.80, CI, 0.51 to 13) versus those who had MRIs more frequently. CONCLUSION: The proposed model can identify high-risk patients, who may benefit from more intensive brain MRI surveillance to reduce morbidity of subsequent treatment through early detection. Wolters Kluwer Health 2022-10-06 /pmc/articles/PMC9848601/ /pubmed/36201713 http://dx.doi.org/10.1200/PO.22.00220 Text en © 2022 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle ORIGINAL REPORTS
Wu, Julie
Ding, Victoria
Luo, Sophia
Choi, Eunji
Hellyer, Jessica
Myall, Nathaniel
Henry, Solomon
Wood, Douglas
Stehr, Henning
Ji, Hanlee
Nagpal, Seema
Hayden Gephart, Melanie
Wakelee, Heather
Neal, Joel
Han, Summer S.
Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes
title Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes
title_full Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes
title_fullStr Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes
title_full_unstemmed Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes
title_short Predictive Model to Guide Brain Magnetic Resonance Imaging Surveillance in Patients With Metastatic Lung Cancer: Impact on Real-World Outcomes
title_sort predictive model to guide brain magnetic resonance imaging surveillance in patients with metastatic lung cancer: impact on real-world outcomes
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9848601/
https://www.ncbi.nlm.nih.gov/pubmed/36201713
http://dx.doi.org/10.1200/PO.22.00220
work_keys_str_mv AT wujulie predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT dingvictoria predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT luosophia predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT choieunji predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT hellyerjessica predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT myallnathaniel predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT henrysolomon predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT wooddouglas predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT stehrhenning predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT jihanlee predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT nagpalseema predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT haydengephartmelanie predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT wakeleeheather predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT nealjoel predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes
AT hansummers predictivemodeltoguidebrainmagneticresonanceimagingsurveillanceinpatientswithmetastaticlungcancerimpactonrealworldoutcomes